Canonical Allele Identifier: CA2319219742

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090612G= , CM000681.2:g.4090612G=	GRCh38
NC_000019.9:g.4090610G= , CM000681.1:g.4090610G=	GRCh37
NC_000019.8:g.4041610G=	NCBI36
NG_007996.1:g.38517C= , LRG_750:g.38517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1628C=
ENST00000688002.1:n.3340C=
ENST00000688751.1:n.325C=
ENST00000689792.1:n.1093C=
ENST00000262948.10:c.1189C= MANE Select	ENSP00000262948.4:p.Arg397=
ENST00000262948.9:c.1189C=	ENSP00000262948.3:p.Arg397=
ENST00000394867.8:c.898C=	ENSP00000378336.1:p.Arg300=
ENST00000597263.5:n.374C=
ENST00000599021.1:c.299C=
ENST00000600584.5:n.2638C=
ENST00000601786.5:n.1490C=
NM_030662.3:c.1189C= , LRG_750t1:c.1189C=	NP_109587.1:p.Arg397=
XM_006722799.2:c.910C=	XP_006722862.1:p.Arg304=
XM_011528133.1:c.619C=	XP_011526435.1:p.Arg207=
NM_030662.4:c.1189C= MANE Select	NP_109587.1:p.Arg397=